Why does 2-propanol (Isopropyl Alcohol) spread more than water on a glass surface?
2-propanol will spread more than water on a glass surface because the surface tension of water is more than that of 2-propanol.
This due to the reason that hydrogen bonding is possible both in 2-propanol and also in water, but the extent of hydrogen bonding is less in 2-propanol compare to water because of the presence of hydrocarbon chain [ CH3CH(OH)CH3 ] but in water no hydrocarbon chain is present so the hydrogen bonding ability will be higher as a result of this water will be having higher surface tension hence the molecules of water stick close together and will not spread much on a glass surface compare to 2-propanol.
Why does 2-propanol (Isopropyl Alcohol) spread more than water on a glass surface?
A bottle of rubbing alcohol contains 75% by mass 2-propanol (C2H8O) in water. What are the mole fractions of 2-propanol and water in the solutions?
Which of the following alcohols would have the lowest solubility in water? A) 1-hexanol B) isopropyl alcohol (2-propanol) C) 1-butanol D) ethanol
3) The temperature of evaporation is much higher for water than for alcohol. Without knowing more about the chemistry of alcohol, which of the following is the most logical chemical explanation for this phenomenon A) Fewer hydrogen bonds form between alcohol molecules. As a result, less heat is needed for alcohol molecules to break away from solution and enter the air. B) Alcohol has a higher surface tension than water. This means that alcohol molecules can easily break away from...
I need the density (g/mL) for the water column and the isopropyl alcohol column. With math shown and included please! The question requires me to show work. If possible, I would also like the percent error's (with work shown) of the water and isopropyl alcohol columns. Thank you! Part 1: Volume and Density Measurements (Liquid) 1 Gather the graduated cylinder, distilled water, short stem pipet, and isopropyl alcohol. 2 Place the clean, dry, 25 ml graduated cylinder on the tared...
Which statement about 2-methyl-1-propanol. (CH),CHCH,OH, and 1,3-propanediol, HOCH,CH,CH,OH is true? 2.Methyl-1-propanol is more soluble in water than 1.3-propanediol because 2-methyl-1-propanol has a smaller molecular mass. 2-Methyl-1-propanol is more soluble in water than 1,3-propanediol because 2-methyl-1-propanol forms fewer hydrogen bonds with water. O 1,3-Propanediol is more soluble in water than 2-methyl-l-propanol because 1,3-propanediol has a smaller molecular mass. O 1,3-Propanediol is more soluble in water than 2-methyl-l-propanol because 1,3-propanediol can form multiple hydrogen bonds with water Draw 2-methylpropanal. Include all hydrogen...
1. Draw the structures of the following alcohols: ethanol 2-propanol cyclohexanol 2-methyl-2-propanol Classify each of the alcohols in question 1 as primary, secondary, or tertiary. ethanol 2-methyl-2-propanol 2. 2-propanol cyclohexanol 3. Which alcohol would you expect to be more soluble in water, 1-butanol or 2-methyl-2- propanol? Why? (Hint: draw both alcohols examine their structures).
A sample of isopropyl alcohol is sealed in a 100.0-cm' glass bulb to which a pressure gauge is (CH CHOHg) is partially dissociated into (CH)Co) and H() according to the equation attached. The bulb d the gauge shows that the pressure in the bulb rises to 0.611 atm At this temperature, the At 179 °C, K-0.444 for this reaction. Assume that the contents of the bulb are at equilibrium and calculate the partial pressure of the three different chemical species...
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19. Which is the best reason for why water in a glass capillary has a concave meniscus, while mercury in a glass capillary has a convex meniscus? A) The water is attracted more strongly to the glass than the mercury is attracted to - the glass. B) Mercury has a greater dispersion force than water. C) Water is a molecular compound while mercury is a metallic element. D) Water has a greater dispersion force than mercury E) Th e mercury...
studying SN1 reactions-oraganic chemistry Prepare a 30 mL solution of 50% isopropyl alcohol solution by mixing together 15 mL isopropyl alcohol and 15 mL water). Divide the solution into three 10 mL portions, placing each one into a 50 mL flask. Add a drop of phenolphthalein indicator to each flask. Add 0.5 M NaOH drop by drop, with swirling, until each mixture is bright pink (this should only take a few drops). Measuring the Effect of the Leaving Group on...